Wits MatCH Research Unit (WMRU), Department of Obstetrics and Gynaecology, Faculty of Health Sciences, University of the Witwatersrand, Durban, South Africa.
Division of Epidemiology and Biostatistics, School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.
BMC Public Health. 2023 Jun 22;23(1):1210. doi: 10.1186/s12889-023-16139-z.
HIV endpoint-driven clinical trials increasingly provide oral pre-exposure prophylaxis (PrEP) as standard of prevention during the trial, however, among participants desiring to continue using PrEP at trial exit, little is known about post-trial PrEP access and continued use.
We conducted one-time, semi-structured, face-to-face, in-depth interviews with 13 women from Durban, South Africa, from November to December 2021. We interviewed women who initiated oral PrEP as part of the HIV prevention package during the Evidence for Contraceptive Options and HIV Outcomes (ECHO) Trial, elected to continue using PrEP at study exit, and were given a 3-month PrEP supply and referred to facilities for PrEP refills at the final trial visit. The interview guide probed for barriers and enablers to post-trial PrEP access, and current and future PrEP use. Interviews were audio-recorded and transcribed. Thematic analysis was facilitated using NVivo.
Of the 13 women, six accessed oral PrEP post-trial exit, but five later discontinued. The remaining seven women did not access PrEP. Barriers to post-trial PrEP access and continued use included PrEP facilities having long queues, inconvenient operating hours, and being located far from women's homes. Some women were unable to afford transport costs to collect PrEP. Two women reported visiting their local clinics and requesting PrEP but were informed that PrEP was unavailable at the clinic. Only one woman was still using PrEP at the time of the interview. She reported that the PrEP facility was located close to her home, staff were friendly, and PrEP education and counselling were provided. Most women not on PrEP reported wanting to use it again, particularly if barriers to access could be alleviated and PrEP was easily available at facilities.
We identified several barriers to post-trial PrEP access. Strategies to enhance PrEP access such as a reduction in waiting queues, convenient facility operating hours, and making PrEP more widely available and accessible are needed. It is also worth noting that oral PrEP access has expanded in South Africa from 2018 till now and this could improve access to PrEP for participants exiting trials who desire to continue PrEP.
艾滋病毒终点驱动的临床试验越来越多地将口服暴露前预防(PrEP)作为试验期间的标准预防措施,但对于在试验结束时希望继续使用 PrEP 的参与者,对于试验后 PrEP 的获取和持续使用知之甚少。
我们于 2021 年 11 月至 12 月在南非德班对 13 名女性进行了一次性、半结构式、面对面的深入访谈。我们采访了在艾滋病毒预防包中作为证据避孕选择和艾滋病毒结局(ECHO)试验的一部分开始使用口服 PrEP 的女性,她们选择在研究结束时继续使用 PrEP,并在最后一次试验访问时获得了 3 个月的 PrEP 供应,并被转介到设施进行 PrEP 续药。访谈指南探究了试验后 PrEP 获取和持续使用的障碍和促进因素,以及当前和未来 PrEP 的使用情况。访谈进行了录音和转录。使用 NVivo 促进了主题分析。
在 13 名女性中,有 6 名在试验结束后获得了口服 PrEP,但其中 5 名后来停止了使用。其余 7 名女性没有获得 PrEP。试验后 PrEP 获取和持续使用的障碍包括 PrEP 设施排队时间长、营业时间不方便、距离妇女家庭较远。一些妇女无法承担收集 PrEP 的交通费用。有两名妇女报告说她们去了当地的诊所并要求 PrEP,但被告知诊所没有 PrEP。只有一名妇女在接受采访时仍在使用 PrEP。她报告说,PrEP 设施离家很近,工作人员很友好,并且提供了 PrEP 教育和咨询。大多数未使用 PrEP 的妇女表示希望再次使用 PrEP,特别是如果可以减轻获取障碍并且 PrEP 在设施中更容易获得。
我们发现了一些试验后 PrEP 获取的障碍。需要采取一些策略来增强 PrEP 的获取途径,例如减少等候队伍、方便设施的营业时间,并使 PrEP 更广泛地可用和可及。值得注意的是,自 2018 年以来,南非的口服 PrEP 获取已经扩大,这可能会改善试验结束时希望继续使用 PrEP 的参与者的 PrEP 获取机会。